C
Cagents13h ago
New
New
EUR 45000–57000/yr
Sterility assurance engineer
OtherEngineer
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Quick Summary
Key Responsibilities
Experience with microbiological and biological methods, including method application and validation. Understanding of quality systems, GMP regulations, and Good Documentation Practices.
Technical Tools
OtherEngineer
CAI Overview:
Are You Ready?
CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field tested processes, and elite expertise developed over 30 years.
Our approach is simple because our Purpose informs everything we do:
· We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.
At CAI, we are committed to living our Foundational Principles, both professionally and personally:
· We act with integrity
· We serve each other
· We serve society
· We work for our future
At CAI, we believe in a relentless dedication to excellence, pushing boundaries and surpassing
expectations. From the beginning, we’ve challenged ourselves to do what others wouldn’t. Not just setting industry standards, but redefining them entirely. We are bold in our thinking and creative in our approach. We operate at the intersection of wisdom and technology and thrive when they come together with humanity. For us, operational readiness isn’t simply a goal. It’s a way of life. Because tomorrow demands to be at the forefront of today. We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement. We’re not interested in how it used to be done. We’re obsessed with how it will be done. Key Responsibilities:
- Experience with microbiological and biological methods, including method application and validation.
- Understanding of quality systems, GMP regulations, and Good Documentation Practices.
- Familiarity with Annex 1 requirements and sterile manufacturing principles.
- Experience with aseptic techniques and biological safety cabinets.
- Ability to work independently while managing multiple priorities.
- Strong attention to detail, organizational skills, and problem-solving capabilities.
Nice to Have
~1 min read- Intermediate level professional with hands-on experience in sterility assurance and aseptic process validation activities.
- Capable of independently managing documentation, coordinating assigned activities, and supporting field execution when required.
- Strong communication and stakeholder management skills.
- Comfortable working in cross-functional and project-based environments.
Requirements
~1 min read- Proficient in spoken and written English.
- Strong technical writing and documentation skills.
- Ability to work autonomously and proactively.
La selezione rispetta il principio delle pari opportunità (l. 903/77)
Location & Eligibility
Where is the job
Italy
Hybrid within the country
Who can apply
Open to applicants worldwide
Listing Details
- Posted
- August 27, 2026
- First seen
- August 27, 2026
- Last seen
- August 27, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 73%
- Scored at
- August 27, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
Salary
EUR 45000–57000
per year
External application · ~5 min on Cagents's site
Please let Cagents know you found this job on Jobera.
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Sterility assurance engineerEUR 45000–57000